Canonical Allele Identifier: PA334270
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 188188
ClinVar RCV Id: RCV000168100 RCV000213342 RCV000663216 RCV001800508 RCV003462256 RCV003987391 RCV003995607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu1335Asp
CA015307
NM_000179.3:c.4005A>C
CA346761626
NM_000179.3:c.4005A>T